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2. Autosomal dominant partial epilepsy with auditory features: A new locus on chromosome 19q13.11–q13.31. Issue 6 (1st March 2014)

3. BRCA-Associated Ovarian Cancer: From Molecular Genetics to Risk Management. (22nd July 2014)

4. Clinical Associations of Biallelic and Monoallelic TNFRSF13B Variants in Italian Primary Antibody Deficiency Syndromes. (30th March 2016)

6. Immune cytopenias as a continuum in inborn errors of immunity: An in‐depth clinical and immunological exploration. Issue 2 (10th April 2021)

7. Italian Registry of Patients with Alpha-1 Antitrypsin Deficiency: General Data and Quality of Life Evaluation. (14th May 2015)

8. Refractory immune thrombocytopenia successfully treated with bortezomib in a child with 22q11.2 deletion syndrome, complicated by Evans syndrome and hypogammaglobulinemia. (4th July 2022)